Anticancer drug development guide : preclinical screening, clinical trials, and approval /

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Bibliographic Details
Edition:2nd ed.
Imprint:Totowa, N.J. : Humana Press, c2004.
Description:xiv, 450 p. : ill. ; 26 cm. + 1 CD-ROM (4 3/4 in.).
Language:English
Series:Cancer drug discovery and development
Subject:
Format: Print Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/5128434
Hidden Bibliographic Details
Other authors / contributors:Teicher, Beverly A., 1952-
Andrews, Paul A.
ISBN:1588292282 (alk. paper)
1592597394 (E-ISBN)
Notes:Includes bibliographical references and index.
System requirements: Serial Number: 4I5Z-29S4-GJ85-NF44

MARC

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505 0 0 |g 1.  |t High-volume screening /  |r Michel Page --  |g 2.  |t High-throughput screening in industry /  |r Michael D. Boisclair, David A. Egan, Kety Huberman and Ralph Infantino --  |g 3.  |t The NCI human tumor cell line (60-cell) screen: concept, implementation, and applications /  |r Michael R. Boyd --  |g 4.  |t Human tumor screening /  |r Axel-R. Hanauske, Susan G. Hilsenbeck and Daniel D. Von Hoff --  |g 5.  |t Murine L1210 and P388 leukemias /  |r William R. Waud --  |g 6.  |t In vivo methods for screening and preclinical testing: use of rodent solid tumors for drug discovery /  |r Thomas Corbett, Lisa Polin, Patricia LoRusso, Fred Valeriote, Chiab Panchapor, Susan Pugh, Kathryn White, Juiwanna Knight, Lisa Demchik, Julie Jones, Lynne Jones and Loretta Lisow --  |g 7.  |t Human tumor xenograft models in NCI drug development /  |r Michael C. Alley, Melinda G. Hollingshead, Donald J. Dykes and William R. Waud --  |g 8.  |t NCI specialized procedures in preclinical drug evaluations /  |r Melinda G. Hollingshead, Michael C. Alley, Gurmeet Kaur, Christine M. Pacula-Cox and Sherman F. Stinson --  |g 9.  |t Patient-like orthotopic metastatic models of human cancer /  |r Robert M. Hoffman --  |g 10.  |t Preclinical models for combination therapy /  |r Beverly A. Teicher --  |g 11.  |t Models for biomarkers and minimal residual tumor /  |r Beverly A. Teicher --  |g 12.  |t Spontaneously occurring tumors in companion animals as models for drug development /  |r David M. Vail and Douglas H. Thamm --  |g 13.  |t Nonclinical testing: from theory to practice /  |r Denis Roy and Paul A. Andrews --  |g 14.  |t Nonclinical testing for oncology drug products /  |r Paul A. Andrews and Denis Roy --  |g 15.  |t Nonclinical testing for oncology biologic products /  |r Carolyn M. Laurencot, Denis Roy and Paul A. Andrews --  |g 16.  |t Working with the national cancer institute /  |r Paul Thambi and Edward A. Sausville --  |g 17.  |t Phase I trial design and methodology for anticancer drugs /  |r Patrick V. Acevedo, Deborah L. Toppmeyer and Eric H. Rubin --  |g 18.  |t Phase II trials: conventional design and novel strategies in the era of targeted therapies /  |r Keith T. Flaherty and Peter J. O'Dwyer --  |g 19.  |t Drug development in europe: the academic perspective /  |r Chris Twelves, Mike Bibby, Denis Lacombe and Sally Burtles --  |g 20.  |t The phase III clinical cancer trial /  |r Ramzi N. Dagher and Richard Pazdur --  |g 21.  |t Assessing tumor-related symptoms and health-related quality of life in cancer clinical trials: a regulatory perspective /  |r Judy H. Chiao, Grant Williams and Donna Griebel --  |g 22.  |t The role of the oncology drug advisory committee in the FDA review process for oncologic products /  |r Leslie A. Vaccari --  |g 23.  |t FDA role in cancer drug development and requirements for approval /  |r Susan Flamm Honig. 
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